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Losartan Latest BP Drug Recalled for Contamination

Losartan Latest BP Drug Recalled for Contamination

Nov. 13, 2018 — Yet any other blood force drug has been recalled as a result of fears of impurities added through a lab in China.

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Drug corporate Sandoz says it has recalled one lot of losartan potassium hydrochlorothiazide drugs. The impurity, referred to as NDEA, was once discovered within the drug’s key factor made through Zhejiang Huahai Pharmaceutical Co. in China.

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NDEA is located naturally in positive meals, ingesting water, air air pollution, and business processes, and it is going to motive most cancers, in line with the International Agency for Research on Cancer.

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The recalled drug may also be known as Losartan Potassium Hydrochlorothiazide, 100-milligram and 25-milligram drugs in 1,000-count plastic bottles; NDC (National Drug Code) 0781-5207-10; Lot quantity JB8912; with an expiration date of 06/2020. This product was once disbursed national to vendors after Oct. eight.

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This newest recall follows a number of others introduced since July, when the FDA introduced the recall of 5 separate valsartan blood force medicine over conceivable NDEA and NDMA contamination. Many extra had been introduced in August because the recall unfold to Canada and the European Union. And previous this month, a blood force drug referred to as irbesartan was once recalled.

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People with questions would possibly touch Sandoz Inc. at 800-525-8747, Monday thru Friday from eight:30 a.m. to five p.m. ET, or electronic mail [email protected] Contact your physician or pharmacist to talk about selection therapies. Patients who’re on losartan must proceed taking their drugs, as they is also much more likely to be harmed if the remedy is stopped with out an alternate.

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Sources

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FDA.gov: “Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API).”

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